METHOD FOR PREPARING RITODRINE HYDROCHLORIDE

Description

[0001] A new method for preparing Ritodrine hydrochloride is object of the present invention. Crystalline polymorphic Ritodrine hydrochloride, Form I, having new and distinctive chemical-physical characteristics, is described, too. Moreover, Ritodrine hydrochloride solvate or monohydrate or Form II are described, from which it has been seen that it is possible to obtain Ritodrine hydrochloride Form I.

Background

[0002] Ritodrine hydrochloride is a pharmaceutical active ingredient classified as beta2-adrenergic agonist, used for its tocolytic action.

[0003] The chemical name of Ritodrine hydrochloride of formula (A) is 4-((1RS,2SR)-1-hydroxy-2-{[2-(4-hydroxyphenyl)ethyl]amino}propyl)phenol hydrochloride.

Legenda = and enantiomer

[0004] Ritodrine hydrochloride is the racemate of the erythro form.

[0005] Ritodrine hydrochloride and its synthesis are described in patent US3410944. In the examples shown in US3410944, Ritodrine hydrochloride is isolated as a solid having a melting point of 183-186°C and 193-195°C. Such different melting points are not compatible with a single polymorphic Ritodrine hydrochloride. The crystalline form of a pharmaceutical active ingredient has an impact on its stability, hygroscopicity, solubility, its dissolution speed and its bioavailability. It is therefore fundamentally important to precisely control the crystalline form of the active ingredient and of the methods to obtain it.

[0006] A different Ritodrine hydrochloride synthesis process is described in EP0492719 and comprises a non-diastereoselective reduction step with sodium borohydride (NaBH4) that provides an erythro/threo mixture 7.5:1, thus obtaining about 12% of undesired isomer mixture.

[0007] EP0603414 describes a stereoselective synthesis for obtaining (-)-Ritodrine hydrochloride and, alternatively, the isolation of (-)-Ritodrine through separation on a chiral column. EP0603414 does not refer to polymorphic forms of the compound.

[0008] Dijk Van J et al, Recueil des Travaux Chimiques des Pays-Bas, vol.92, no.12, (1973), pages 1281-1297, describes the preparation of Ritodrine HCl starting from the erythro intermediate obtained in turn starting from the erythro form of the alcohol. The last step of the synthesis involves the removal of a benzyl-protecting group by catalytic hydrogenation. The described yield is poor (73%).

Summary of the invention

[0009] In the present invention a method to provide Ritodrine hydrochloride in a crystalline form that is well defined and stable, hereafter called Form I is described.

[0010] Ritodrine hydrochloride Form I can be obtained according to the following methods:

(i) treating Ritodrine hydrochloride in alcoholic solvent with one or more organic solvents and subsequent precipitation of Ritodrine hydrochloride Form I;

(ii) transforming Ritodrine hydrochloride solvate or monohydrate or Form II, by suspension in organic solvents, and the subsequent separation of Ritodrine hydrochloride Form I;
or

(iii) transforming Ritodrine hydrochloride solvate or monohydrate or Form II by drying to obtain Ritodrine hydrochloride Form I.

[0011] Ritodrine hydrochloride Form I is advantageous since it is stable and it is non-hygroscopic.

[0012] The purpose of the invention is to obtain Ritodrine hydrochloride through a new synthesis process that provides Ritodrine hydrochloride with high yield and purity.

[0013] Such a preparation method of Ritodrine hydrochloride foresees:

(a) the reaction of 4-(2-bromopropionyl)phenyl methanesulfonate with benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amine to obtain 4-(2-{benzyl-[2-(4-benzyloxy-phenyl)-ethyl]-amino}-propionyl)-phenyl methanesulfonate (B).

(b) the hydrolysis of the product obtained in (a) in the corresponding deprotected form 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one (C).

(c) the salification of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one (C).

(d) the catalytic hydrogenation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D) so as to obtain Ritodrine hydrochloride (A).

Legenda = and enantiomer

[0014] Further characteristics and advantages of the method according to the invention shall become clearer from the following description and from the preferred embodiments, given as an example and not for limiting purposes.

[0015] A more complete understanding of the present invention can be obtained by referring to the tables summarising some chemical-physical characteristics for the compounds named in the rest of the description.

[0016] Ritodrine hydrochloride, Form I, Ritodrine hydrochloride, Form II, Ritodrine hydrochloride solvated with acetone, Ritodrine hydrochloride solvated with ethyl acetate, Ritodrine hydrochloride monohydrate for which the main x-ray diffraction peaks, the main and characteristic bands of the IR spectrum and the main and characteristic bands of the Raman spectrum, are shown.

[0017] The x-ray powder diffractogram (XRPD) was obtained by using a CuKα1 radiation. The diffractogram is measured in reflection modality in the range of 5-40°2θ.

[0018] The IR spectrum was acquired in ATR modality (Attenuated Total Reflection) and it is measured in cm^-1.

[0019] The Raman spectrum was acquired by using a laser source of 400mW operating at 785 nm and it is measured in cm^-1.

Detailed description of the invention

[0020] It has surprisingly been found that Ritodrine hydrochloride exists in two polymorphic forms, Form I and Form II, having very distinct chemical-physical properties. Ritodrine hydrochloride Form I is particularly advantageous with respect to Form II since it is non-hygroscopic. In virtue of this non-hygroscopicity, the chemical-physical properties of Ritodrine hydrochloride Form I can be controlled more easily. All of this is fundamentally important when Ritodrine hydrochloride is formulated.

[0021] Vice versa, Ritodrine hydrochloride Form II is hygroscopic. As it is well known in the pharmaceutical industry, the formulation of hygroscopic active ingredients foresees the use of rooms with controlled humidity during the storage and the formulation itself. Moreover, the formulated product must be packaged in a suitable manner so as to avoid problems of stability due to humidity. These problems are avoided when non-hygroscopic Ritodrine hydrochloride Form I is used.

[0022] Ritodrine hydrochloride Form I is characterised in that it is non-hygroscopic and stable in its water content as measured through Karl Fischer titration. It has surprisingly been found that Ritodrine hydrochloride Form I does not absorb water even when it is exposed to a relative humidity of 75%.

[0023] In the present application, by the term "non-hygroscopic" we mean that Ritodrine hydrochloride Form I absorbs less than 1% of water, like for example less than 0.5%, when it is exposed to an environment with 75% relative humidity.

[0024] Vice versa, Ritodrine hydrochloride Form II absorbs water even when it is not exposed directly to a humid environment but in normal controlled storing conditions like those foreseen for active ingredients.

[0025] In particular Ritodrine hydrochloride Form I described in the present invention is a crystalline solid characterised as follows:

Table 1:

XRPD	IR	RAMAN
2θ (°)	cm-1	cm-1
4.87	3380	3058
9.24	3012	3015
12.52	2854	2982
14.15	2827	2944
15.17	1612	2863
15.71	1595	1615
16.49	1514	1600
18.06	1443	1596
18.51	1402	1449
19.20	1388	1364
19.67	1354	1339
20.41	1342	1320
21.64	1326	1291
23.04	1291	1265
24.08	1261	1205
24.94	1203	1173
25.71	1172	1129
26.12	1128	1114
26.48	1115	1095
27.18	1098	1077
29.48	1076	1048
33.22	1048	1030
33.55	1031	1017
35.01	1015	993
35.32	992	969
	969	922
	874	848
	856	824
	832	713
	809	668
	790	641
	763	598
	718	481
	667	406
		390
		341

[0026] Ritodrine hydrochloride Form II is a crystalline solid characterised as follows:

Table 2:

XRPD	IR	RAMAN
2θ(°)	cm-1	cm-1
9.35	3411	3057
12.52	3270	3016
14.06	3008	2946
15.14	2843	2911
15.76	2440	2879
16.31	1889	2864
17.55	1614	1616
18.74	1594	1602
19.02	1577	1594
19.69	1516	1448
20.42	1446	1419
20.64	1393	1321
21.46	1358	1290
22.36	1263	1265
23.88	1222	1208
24.94	1173	1139
26.97	1138	1073
28.25	1116	1046
31.81	1093	1014
32.53	1073	992
34.14	1046	926
37.97	1013	879
	993	848
	879	825
	834	718
	814	642
	792	472
	777	449
	717	394
	661	362
		351
		243

[0027] Ritodrine hydrochloride Form I can be obtained according to the following methods:

(i) treating Ritodrine hydrochloride in alcoholic solvent with one or more organic solvents so as to obtain a solution and subsequent precipitation of Ritodrine hydrochloride Form I;
or

(ii) transforming Ritodrine hydrochloride solvate or monohydrate or Form II, by suspension in organic solvents, and the subsequent separation of Ritodrine hydrochloride Form I;
or

(iii) transforming Ritodrine hydrochloride solvate or monohydrate or Form II, by drying so as to obtain Ritodrine hydrochloride Form I.

[0028] In another embodiment of the present invention Ritodrine hydrochloride is obtained according to a method that comprises:

(a) the reaction of 4-(2-bromopropionyl)phenyl methanesulfonate with benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amine to obtain 4-(2-{benzyl-[2-(4-benzyloxy-phenyl)-ethyl]-amino}-propionyl)-phenyl methanesulfonate (B).

(b) the hydrolysis of the product obtained in (a) in the corresponding deprotected form 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one of formula (C).

(c) the salification of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one (C).

(d) the catalytic hydrogenation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride of formula (D) and subsequent concentration, following the separation of the catalyst, through low pressure distillation, so as to obtain Ritodrine hydrochloride (A).

[0029] In step (a) 4-(2-bromopropionyl)phenyl methanesulfonate is obtained through bromination of 4-propionyl-phenyl methanesulfonate with bromine. 4-(2-bromopropionyl)phenyl methanesulfonate is subsequently made to react with benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino in base presence to obtain the methane sulfonic ester 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-oxy-phenyl)-propan-1-one (B).

[0030] In one embodiment, the hydrolysis of the methane sulfonic ester of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-oxy-phenyl)-propan-1-one (B) in step (b) is carried out by means of a base that can be, as an example and not for limiting purposes, a hydroxide of alkaline and/or alkaline earth metals, typically potassium hydroxide or sodium hydroxide in a solvent formed by mixtures of acetone-water, methyl ethyl ketone-water or mixtures thereof. The compound (C) obtained is thus isolated through crystallization by acetone, methyl ethyl ketone, mixtures of acetone-water, methyl ethyl ketone-water or mixtures thereof.

[0031] In step (c) 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl ]-amino}-1-(4-hydroxy-phenyl)-propan-1-one (C) is salified with a suitable acid. In one embodiment, the compound (C) is transformed into its corresponding hydrochloride salt (D) by using hydrochloric acid, gaseous or in solution, in a solvent that is selected, as an example and not for limiting purposes, amongst toluene, ethanol, methanol, water, acetone, methyl ethyl ketone, ethyl acetate or mixtures thereof.

[0032] Alternatively, a direct conversion of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-oxy-phenyl)-propan-1-one methanesulfonate (B) in the salified form 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one (D) is carried out, without isolation of the free base (C).

[0033] In step (d) through treatment with hydrogen in presence of a catalyst, 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D) is converted into the corresponding compound 4-((1RS,2SR)-1-hydroxy-2-{[2-(4-hydroxyphenyl)ethyl]amino}propyl)phenol hydrochloride (Ritodrine hydrochloride) (A). In one embodiment, the catalytic hydrogenation of (D) occurs by using a catalyst made up of a palladium on carbon (Pd/C) in an organic solvent, preferably in alcohol or in alcohol mixed with water. As an example the alcohol is selected amongst methanol or ethanol or mixtures thereof.

[0034] The hydrogenation reaction is carried out in a hydrogen atmosphere according to what is known by a man skilled in the art and in particular with a pressure that is preferably comprised between 2 and 12 bar and at temperatures comprised between 20°C and 45°C. In such conditions, and differently from what is shown in EP0492719, the reaction is very selective and provides an erythro/threo mixture of about 98:2.

[0035] The solution of Ritodrine hydrochloride obtained from the hydrogenation reaction, following filtration of the catalyst, is concentrated through low pressure distillation.

[0036] Ritodrine hydrochloride in alcoholic solvent obtained from the hydrogenation reaction is subsequently diluted with ethers or aliphatic hydrocarbons such as methyl-tert-butyl ether, heptane or mixtures thereof or methyl ethyl ketone until the precipitation of Ritodrine hydrochloride is obtained. The solid is isolated through filtration.

[0037] The humid solid thus obtained has the desired crystalline form, Form I. In a further embodiment, Ritodrine hydrochloride in alcoholic solvent used to obtain Form I, as described above, is obtained by mixing solid Ritodrine hydrochloride with an alcoholic solvent.

[0038] In another aspect of the present invention, the solution of Ritodrine hydrochloride obtained by the hydrogenation reaction, after filtration of the catalyst and subsequent concentration through low pressure distillation, is precipitated as a solvated form through treatment with suitable organic solvents.

[0039] In a further embodiment, Ritodrine hydrochloride in alcoholic solvent, used to obtain the solvate, is obtained by mixing solid Ritodrine hydrochloride with alcoholic solvent and subsequent precipitation through treatment with suitable organic solvents.

[0040] Suitable organic solvents used for the precipitation of Ritodrine hydrochloride solvate comprise acetone, ethyl acetate or mixtures thereof. The precipitation of Ritodrine hydrochloride can be possibly primed. The isolation of Ritodrine hydrochloride as a solved form is very advantageous since it provides Ritodrine hydrochloride with high chemical purity. The product obtained is Ritodrine hydrochloride solvate with a chemical purity that is greater than 98%, typically greater than 99% or greater than 99.8%.

[0041] One example of Ritodrine hydrochloride solvate is the solvate with acetone, which is characterised as follows:

Table 3:

XRPD	IR	RAMAN
2θ (°)	cm-1	cm-1
3.75	3262	3061
7.49	3004	3018
11.50	2952	3004
14.24	2820	2954
14.98	2431	2856
16.29	1698	1692
17.35	1615	1618
19.02	1593	1600
20.32	1564	1549
21.06	1548	1478
21.65	1515	1446
22.42	1454	1424
23.23	1390	1305
24.06	1367	1290
24.87	1310	1266
25.30	1290	1213
25.80	1263	1196
26.38	1236	1168
26.93	1217	1153
32.15	1191	1118
35.48	1169	1075
	1151	1052
	1118	1020
	1097	993
	1075	928
	1053	885
	1020	848
	993	815
	959	798
	936	765
	908	717
	885	658
	872	642
	843	580
	829	546
	815	343
	789
	765
	718
	660

[0042] A further example of Ritodrine hydrochloride solvate is the solvate with ethyl acetate, which is characterised as follows:

Table 4:

XRPD	IR	RAMAN
2θ (°)	cm-1	cm-1
7.37	3338	3062
7.87	3101	3017
9.01	2979	2982
14.73	2799	2944
15.75	2465	2873
16.43	1742	1735
16.62	1730	1617
17.09	1615	1602
17.85	1595	1546
18.67	1579	1449
19.39	1546	1411
19.69	1514	1285
20.60	1441	1265
20.88	1410	1207
21.91	1392	1185
22.27	1372	1174
22.73	1342	1152
23.66	1264	1115
24.19	1220	1107
25.19	1171	1072
26.18	1150	1044
27.12	1115	1012
30.70	1090	928
	1070	884
	1043	848
	1010	823
	991	776
	938	718
	882	654
	847	642
	829	635
	791	473
	767	447
	714	382
	656	354
		205

[0043] In another aspect of the present invention, the solution of Ritodrine hydrochloride obtained by the hydrogenation reaction, after filtration of the catalyst and subsequent concentration through low pressure distillation, is precipitated as a monohydrate through treatment with an aqueous solution. The precipitation of Ritodrine hydrochloride can be possibly primed. The mixture thus obtained is left to crystallise keeping it under stirring at a temperature comprised between 15°C and 30°C, preferably at 20°C for a time of from 4 to 48 hours, preferably from 10 to 24 hours.

[0044] Ritodrine hydrochloride monohydrate is obtained by mixing solid Ritodrine hydrochloride and an aqueous solution.

[0045] The compound obtained in such conditions is Ritodrine hydrochloride monohydrate with a chemical purity that is greater than 98%, typically greater than 99% or greater than 99.8%. Ritodrine hydrochloride monohydrate is characterised as follows:

Table 5:

XRPD	IR	RAMAN
2θ (°)	cm-1	cm-1
3.77	3479	3093
7.51	3407	3060
11.50	3187	3015
14.24	3052	2989
15.00	2977	2962
16.27	2825	2947
17.37	2685	2915
19.02	2602	2887
20.33	2448	2865
20.75	1614	1616
21.08	1601	1602
21.66	1568	1577
22.35	1515	1476
23.26	1453	1446
23.85	1373	1427
24.08	1353	1389
24.87	1314	1368
25.31	1294	1312
25.78	1278	1295
26.37	1230	1279
26.92	1175	1258
28.67	1127	1216
	1099	1205
	1071	1189
	1044	1132
	1010	1109
	985	1072
	964	1041
	903	1015
	882	987
	851	943
	826	903
	809	883
	785	855
	753	831
	716	827
	701	809
	655	789
		718
		639
		570
		524
		450
		420
		390
		357

[0046] The water content of Ritodrine hydrochloride monohydrate determined through Karl Fischer titration is 5.3% (weight/weight) and is congruous with the presence of one molecule of water in the crystal lattice.

[0047] It has been observed that Ritodrine hydrochloride Form I can be obtained even from other crystalline forms of Ritodrine hydrochloride like the solvate, the monohydrate and Form II. In one aspect the transformation occurs wet, by suspension in organic solvents, and the subsequent separation of Ritodrine hydrochloride Form I. In a further aspect the suspension of Ritodrine hydrochloride solvate, monohydrate or From II, is carried out in ethers or aliphatic hydrocarbons such as methyl-tert-butyl ether, or heptane, or methyl ethyl ketone or mixtures thereof.

[0048] The suspension in such solvents is carried out through stirring at a temperature greater than 0°C, preferably between 20°C and the boiling point of the solvent and even more preferably at a temperature comprised between 30°C and 50°C for at least 1 hour.

[0049] The transformation of Ritodrine hydrochloride in the desired form, Form I, can be monitored by using suitable methods that are known by a man skilled in the art.

[0050] In another aspect the transformation occurs dry. It has been observed that Ritodrine hydrochloride solvate or monohydrate or Form II, is transformed into Ritodrine hydrochloride Form I through a drying process. It has been observed that such transformations occur at specific temperatures and over specific amounts of time. When these conditions are not scrupulously applied, Ritodrine hydrochloride is, instead, obtained as Form II, or as a mixture of Form I and Form II. It is obvious that the presence of Form II in the active ingredient is not desired. The transformation in dry conditions of Ritodrine hydrochloride Form I occurs by acting at a temperature of at least 60°C and preferably at temperatures of between 75°C and 85°C for at least 1 hour.

[0051] The transformation of Ritodrine hydrochloride into the desired form, Form I, can be monitored by using suitable methods that are known by a man skilled in the art. The transformation in dry conditions of Ritodrine hydrochloride Form I can occur even at temperatures that are greater than 85°C but with partial decomposition of the compound with the formation of by-products such as tyramine causing there to be reduced chemical purity of the active ingredient.

[0052] The chemical purity of Ritodrine hydrochloride can be increased even through a process of

a') recrystallization with complete dissolution; or

b') resuspension in organic solvents without reaching complete dissolution;

followed by the separation of the solid which is Ritodrine hydrochloride.

[0053] In the examples that follow the application of the present invention is illustrated.

Experimental part

[0054] X-ray powder diffractograms (XRPD) were obtained by using a CuKα1 radiation. The diffractograms were measured in reflection modality in the range 5-40°2θ.

[0055] The IR spectrums were acquired in ATR (Attenuated Total Reflection) modality and measured in cm^-1.

[0056] The Raman spectrums were acquired by using a laser source of 400 mW operating at 785 nm and measured in cm^-1.

[0057] The water content was determined through Karl Fischer (KF) titration.

Example 1: - Preparation of 4-(2-{benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)phenyl methanesulfonate (B).

[0058] 100g of 4-propionyl-phenyl methanesulfonate and 360 ml of dichloromethane were loaded into a 2 litre reactor. The solution obtained was cooled to 0°C and, at such a temperature, 3g of solution with 33% of Hbr in acetic acid and subsequently 23 ml of Br₂ (71.6g) were added. Once these were added, the solution obtained was left under stirring for 1 hour at a temperature of around 0°C.

[0059] 200ml of H₂O were added to the solution, then the mass was heated to 20°C and kept at such a temperature for 30 minutes.

[0060] Once the stirring had stopped the two phases were separated and the organic phase was reloaded on the reactor and 260 ml of ethanol were added to it.

[0061] The solution obtained was heated to around 80°C progressively distilling the dichloromethane, then cooled to 40°C and diluted with 1780 ml of ethanol.

[0062] 133.2 g of benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amine and subsequently 104 ml of triethylamine were added to it under stirring. The mass was heated to reflux and was kept at reflux for about 18 hours, then it was gradually cooled down to room temperature, obtaining a suspension that was then filtered.

[0063] The crystalline solid obtained was vacuum dried at 60°C for 10 hours.

[0064] 195 g of 4-(2-{benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)phenyl methanesulfonate (B) were obtained.

[0065] Molar yield 82%, purity 97.5% HPLC (A%).

Example 2:

4-(2-{benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)phenyl methanesulfonate (B).

[0066] 100g of 4-(2-bromopropionyl)-phenyl methanesulfonate and 1750 ml of ethanol were loaded into a 3 litre reactor.

[0067] 103 g of benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino and after 77 ml of triethylamine were added to it under stirring. The mass was heated to reflux and kept at reflux for about 18 hours, then it was gradually cooled down to room temperature, obtaining a suspension that was then filtered.

[0068] The crystalline solid obtained was vacuum dried at 60°C for 10 hours.

[0069] 148.96 g of 4-(2-{benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)phenyl methanesulfonate (B) were obtained.

[0070] Molar yield 84%, purity 98.4% HPLC (A%).

Example 3: Preparation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one (C).

[0071] 50 g of 4-(2-{benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)phenyl methanesulfonate (B), 100 ml of water, 355 ml of acetone and 18.4 g of potassium hydroxide are introduced into a one litre glass reactor at room temperature. The mixture is heated to reflux temperature (about 59°C) and kept at such a temperature for two hours. Subsequently, the mixture is cooled down to 45-50°C and 30% hydrochloric acid is added until a pH of around 7 is obtained. The lower phase is separated and the organic phase is diluted with 100 ml of water. A suspension is obtained that is cooled down to 0°C. The solid is isolated through filtration and washed and then vacuum dried at 40°C. 41.4 g of 2-{Benzyl-[2-(4-benzyloxy-phenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one (C) as a white solid, are obtained.

[0072] Molar yield 96%, chemical purity 99.63% HPLC (A%).

Example 4: - Preparation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D).

[0073] 20 g of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one and 100 ml of methyl ethyl ketone are introduced into a 250 ml reactor. At 20°C, 9g of a solution with 19% by weight of HCl in 2-butanone are added. Once the precipitation of the solid has occurred, it is heated to 50°C and it is diluted with 40 ml of methyl ethyl ketone. It is kept under stirring for an hour and then it is cooled down again to 20°C. The solid is filtered and is washed with 80 ml of methyl ethyl ketone. After vacuum drying at 40°C, 20.6 g of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride as a white solid, are obtained.

[0074] Molar yield 95%, chemical purity: 99.76% HPLC (A%).

Example 5: - Preparation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D).

[0075] 400g of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one and 2000 ml of acetone are loaded into a one litre glass reactor, at room temperature. Keeping the temperature at 20°C, 34.8 g of gaseous hydrochloric acid is injected. Once the acid has been added it is primed with 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride, obtaining the precipitation of the product. The suspension is kept under stirring at 20°C over night. The product is finally isolated through filtration, washed with 200 ml of acetone and vacuum dried at 40°C. 413 g of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride as a white solid, are obtained.

[0076] Molar yield 95%, chemical purity 99.84% HPLC (A%)

Example 6: - Preparation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D).

[0077] A 500 ml reactor was loaded with 20 g of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one, 200 ml of toluene and 10 ml of ethanol. The suspension thus obtained was brought to the temperature of 50°C and at such a temperature, under stirring, 4 ml of 37% HCl were added, observing the complete dissolution of the suspended solid.

[0078] The solution was then cooled down first to 32°C and then to 0°C. The solid obtained through crystallization was filtered, washed with 15 ml of isopropanol and vacuum dried at 55°C.

[0079] 21 g of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D) were obtained as a white solid.

[0080] Molar yield 97%, purity 99.66% HPLC (A%).

Example 7: Hydrogenation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D).

[0081] A 5 litre steel autoclave is loaded with 130 g of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D), 481 ml of methanol and 4.6 g of 5% palladium on carbon. The mixture is heated to 30°C and keeping the pressure at 6 bar hydrogen is injected until there is zero absorption. The mixture is filtered to remove the catalyst obtaining 504 g of alcoholic solution of Ritodrine hydrochloride.

[0082] Chemical purity (area, HPLC): Ritodrine hydrochloride 98.1%; threo isomers 1.3%.

Example 8: Hydrogenation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D).

[0083] A 5 litre steel autoclave is loaded with 716 g of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride (D), 2650 ml of absolute ethanol and 107.7 g of 5% palladium on carbon 60% humid. The mixture is heated to 40°C and keeping the pressure at 6 bar, hydrogen is injected until there is zero absorption. The mixture is filtered to remove the catalyst obtaining 2778 g of alcoholic solution of Ritodrine hydrochloride. Chemical purity (area, HPLC): Ritodrine hydrochloride 98.1%; threo isomers 1.2%.

Example 9(illustrative example only): 4-((1RS,2SR)-1-hydroxy-2-{[2-(4-hydroxyphenyl)ethyl]amino}propyl)phenol hydrochloride (Ritodrine hydrochloride) Form I.

[0084] A methanolic solution of Ritodrine hydrochloride obtained as described in example 8 in which it is estimated that there are 58 g of product, is concentrated as a residue and is diluted with 89 ml of methanol. The solution thus obtained is treated with 1180 ml of methyl-tert-butyl ether and heated to 37°C obtaining a suspension. It is stirred for 11 hours and then cooled down to 20°C, it is filtered and the solid is washed with methyl-tert-butyl ether. It is vacuum dried at 40°C obtaining 76.8 g of Ritodrine hydrochloride. The X-ray diffraction pattern corresponds to that of Ritodrine hydrochloride Form I shown in table 1.

Example 10 (illustrative example only): - 4-((1RS,2SR)-1-hydroxy-2-{[2-(4-hydroxyphenyl)ethyl]amino}propyl)phenol hydrochloride (Ritodrine hydrochloride) solvated with acetone.

[0085] A methanolic solution of Ritodrine hydrochloride obtained as described in example 8 in which it is estimated that there are around 65 g of Ritodrine hydrochloride are concentrated as a residue through low pressure distillation. The residue is diluted with 10 ml of methanol and 650 ml of acetone. The mixture is brought to 37°C and is kept under stirring at 37°C for 11 hours. It is cooled down to room temperature and the product is isolated through filtration. It is washed with 200 ml of acetone and 102 g of Ritodrine hydrochloride are obtained. Chemical purity: 99.84% HPLC (A%). The X-ray diffraction pattern corresponds to that of Ritodrine hydrochloride solvated with acetone shown in table 3.

Example 11 (illustrative example only): - 4-((1RS,2SR)-1-hydroxy-2-{[2-(4-hydroxyphenyl)ethyl]amino}propyl)phenol hydrochloride (Ritodrine hydrochloride) solvated with ethyl acetate.

[0086] 100 g of an ethanolic solution of Ritodrine hydrochloride obtained according to the method described in example 8, containing about 15 g of Ritodrine hydrochloride, are concentrated by vacuum distilling 50 g of solvent. The solution thus obtained is cooled down to 0°C. 200 ml of ethyl acetate are dripped obtaining the precipitation of the product. The suspension is kept under stirring over night at 0°C. The solid is filtered. 14.5 g of Ritodrine hydrochloride are obtained.

[0087] Chemical purity: 99.25% HPLC (A%). The X-ray diffraction pattern corresponds to that of Ritodrine hydrochloride solvated with ethyl acetate shown in table 4.

Example 12 (illustrative example only): - 4-((1RS,2SR)-1-hydroxy-2-{[2-(4-hydroxyphenyl)ethyl]amino}propyl)phenol hydrochloride (Ritodrine hydrochloride) monohydrate.

[0088] 25 g of Ritodrine hydrochloride is suspended in 50 ml of water and is kept stirred at 20°C for 20 hours. It is then cooled down to 0°C in about an hour and it is kept at 0°C for 3 hours.

[0089] The solid is filtered and is vacuum dried at 50°C for 24 hours. 21 g of Ritodrine hydrochloride monohydrate are obtained.

[0090] The X-ray diffraction pattern is the same as that of Ritodrine hydrochloride monohydrate shown in table 5.

Example 13 (illustrative example only): - Transformation of Ritodrine hydrochloride solvated with acetone into Ritodrine hydrochloride Form I.

[0091] 20 g of Ritodrine hydrochloride solvated with acetone obtained as described in example 10 are suspended in 40 ml of methyl-tert-butyl ether. The suspension is kept stirred at 50°C-55°C for 3 hours and is then cooled down to 20°C. It is filtered and washed with methyl-tert-butyl ether and is vacuum dried at 50°C.

[0092] 13.3 g of Ritodrine hydrochloride Form I are obtained.

Example 14 (illustrative example only): - Transformation of Ritodrine hydrochloride solvated with acetone into Ritodrine hydrochloride Form I.

[0093] 20 g of Ritodrine hydrochloride solvated with acetone obtained as described in example 10 are suspended in 100 ml of heptane. The suspension is heated to reflux temperature for 1-1.5 hours and is then cooled down to 20°C. The solid is filtered and is vacuum dried at 50°C. 13.8 g of Ritodrine hydrochloride Form I are obtained.

Example 15 (illustrative example only): - Transformation of Ritodrine hydrochloride monohydrate into Ritodrine hydrochloride Form I.

[0094] Ritodrine hydrochloride monohydrate is placed to vacuum dry in an oven at a temperature of 80°C for 12 hours. Ritodrine hydrochloride Form I is obtained.

Example 16 (illustrative example only): - Transformation of Ritodrine hydrochloride solvated with ethyl acetate into Ritodrine hydrochloride Form I.

[0095] Ritodrine hydrochloride solvated with ethyl acetate is placed to vacuum dry in an oven at a temperature of 80°C for 26 hours. Ritodrine hydrochloride Form I is obtained.

Example 17 (illustrative example only): - Preparation of Ritodrine hydrochloride Form II.

[0096] Ritodrine hydrochloride solvated with acetone is placed to vacuum dry in an oven at a temperature of 40°C for 22 hours. Ritodrine hydrochloride Form II is obtained. The X-ray diffraction pattern corresponds to that of Ritodrine hydrochloride Form II shown in table 2.

Example 18 (illustrative example only): - Transformation of Ritodrine hydrochloride Form II into Ritodrine hydrochloride Form I.

[0097] Ritodrine hydrochloride Form II is placed to vacuum dry in an oven at a temperature of 80°C for 17 hours. Ritodrine hydrochloride Form I is obtained.

Example 19 (illustrative example only): - Recrystallization of Ritodrine hydrochloride.

[0098] 100 g of Ritodrine hydrochloride are suspended at room temperature in 300 ml of methyl ethyl ketone. 80 ml of methanol are added obtaining a solution that is subsequently heated to 37°C and diluted with 700 ml of methyl ethyl ketone. The precipitation is started by adding a primer. The suspension is kept at 37°C for 4 hours and is then left to cool down to room temperature. It is filtered and washed with 200 ml of methyl ethyl ketone. The solid is vacuum dried at 60°C obtaining 60 g of Ritodrine hydrochloride Form I. Chemical purity 99.9% HPLC (A%).

Example 20 (illustrative example only): - Stability of Ritodrine hydrochloride Form I.

[0099] Ritodrine hydrochloride Form I is kept at 40°C and a relative humidity of 75% for 24 hours. The water content measured through Karl Fischer titration is 0.5% (weight/weight).

Example 21 (illustrative example only) : - Stability of Ritodrine hydrochloride Form II.

[0100] Ritodrine hydrochloride Form II is placed in a double polyethylene bag with a desiccant (silica gel) kept in standard conditions for storing active ingredients. After some months the water content of such Ritodrine hydrochloride measured through Karl Fischer titration is 2.2% (weight/weight).

Claims

1. Method for preparing Ritodrine hydrochloride comprising:

(a) the reaction of 4-(2-bromopropionyl)phenyl methanesulfonate with benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amine to obtain 4-(2{benzy1-[2-(4-benzyloxy-methanesulfonate.

(b) the hydrolysis of 4-(2-{benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)-phenyl Methanesulfonate to obtain 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one.

(c) the salification of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one.

(d) the catalytic hydrogenation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride to obtain Ritodrine hydrochloride.

2. Method according to claim 1, wherein the hydrolysis in (b) is performed by means of a base, wherein the base is an alkaline metal and/or earth alkaline hydroxide, potassium hydroxide or sodium hydroxide in a solvent made of mixtures of acetone-water, methyl ethyl ketone-water or mixtures thereof.

3. Method according to claim 2, wherein 2-{Benzyl-[2 (4-benzyloxyphenyl)-ethyl]-amino}-1-(4- hydroxy-phenyl)-propan-1-one is isolated by crystallisation from acetone, methyl ethyl ketone, mixtures of acetone-water, methyl ethyl ketone-water or mixtures thereof.

4. Method according to claim 1, wherein the salification occurs by using hydrochloric acid, gaseous or in solution, in an organic solvent, wherein the organic solvent is toluene or ethanol or methanol or water or acetone or methyl ethyl ketone or ethyl acetate or mixtures thereof.

5. Method according to claim 1, wherein the catalytic hydrogenation of 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride occurs by using a catalyst constituted by palladium on carbon (Pd/C) in an organic solvent, wherein the organic solvent is an alcohol or an alcohol mixed with water, in a hydrogen atmosphere comprised between 2 and 12 bars, at temperatures comprised between 20°C and 45°C.

6. The compound

- 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one or its hydrochloride salt.

7. The compound

4-(2-{benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)-phenyl methanesulfonate.

8. The compound according to claim 6, of formula:

- 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-one hydrochloride.

Ansprüche

1. Verfahren zur Herstellung von Ritodrin-Hydrochlorid, umfassend:

(a) Reaktion von 4-(2-Brompropionyl)-phenyl-methansulfonat mit Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amin zur Gewinnung von 4-(2-{Benzyl-[2-(4-benzyloxy-phenyl)-ethyl]-amino}-propionyl)-phenyl-methansulfonat,

(b) Hydrolyse von 4-(2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)-phenyl-methansulfonat zur Gewinnung von 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-on,

(c) Salzbildung von 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-on,

(d) katalytische Hydrierung von 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-on-hydrochlorid zur Gewinnung von Ritodrin-Hydrochlorid.

2. Verfahren nach Anspruch 1, wobei die Hydrolyse in (b) mit Hilfe einer Base, wobei die Base ein Alkalimetall- und/oder Erdalkalimetallhydroxid, Kaliumhydroxid oder Natriumhydroxid ist, in einem Lösungsmittel, hergestellt aus Gemischen aus Aceton-Wasser, Methylethylketon-Wasser oder Gemischen davon, ausgeführt wird.

3. Verfahren nach Anspruch 2, wobei 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-on durch Kristallisation aus Aceton, Methylethylketon, Gemischen aus Aceton-Wasser, Methylethylketon-Wasser oder Gemischen davon isoliert wird.

4. Verfahren nach Anspruch 1, wobei die Salzbildung durch Anwendung von Chlorwasserstoffsäure, gasförmig oder in Lösung, in einem organischen Lösungsmittel stattfindet, wobei das organische Lösungsmittel Toluol oder Ethanol oder Methanol oder Wasser oder Aceton oder Methylethylketon oder Essigsäureethylester oder Gemische davon ist.

5. Verfahren nach Anspruch 1, wobei die katalytische Hydrierung von 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-on-hydrochlorid durch Anwendung eines aus Palladium-auf-Kohlenstoff (Pd/C) erzeugten Katalysators in einem organischen Lösungsmittel, wobei das organische Lösungsmittel ein Alkohol oder ein mit Wasser gemischter Alkohol ist, in einer Wasserstoffatmosphäre, umfasst zwischen 2 und 12 bar, bei Temperaturen, umfasst zwischen 20°C und 45°C, stattfindet.

6. Verbindung

- 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-on oder sein Hydrochloridsalz.

7. Verbindung

- 4-(2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-propionyl)-phenyl-methansulfonat.

8. Verbindung nach Anspruch 6, der Formel:

- 2-{Benzyl-[2-(4-benzyloxyphenyl)-ethyl]-amino}-1-(4-hydroxy-phenyl)-propan-1-on-hydrochlorid.

Revendications

1. Procédé pour la préparation de chlorhydrate de ritodrine comprenant :

(a) la réaction de 4-(2-bromopropionyle)méthanesulfonate de phényle avec du benzyle-[2-(4-benzyloxyphényle)-éthyle]-amine pour obtenir du 4-(2-{benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}-propionyle)-méthanesulfonate de phényle.

(b) l'hydrolyse du 4-(2{benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}-propionyle)-méthanesulfonate de phényle pour obtenir du 2- -{benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}-1-(4-hydroxy-phényle)-propan-1-one.

(c) la salification du 2-{benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}-1-(4-hydroxy-phényle)-propan-1-one.

(d) l'hydrogénation catalytique du chlorhydrate de 2- {benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}--1-(4-hydroxy-phényle)-propan-1-one pour obtenir du chlorhydrate de ritodrine.

2. Procédé selon la revendication 1, caractérisé en ce que l'hydrolyse du (b) est réalisée à l'aide d'une base, dans laquelle la base est un métal alcalin et/ou un hydroxyde alcalino-terreux, un hydroxyde de potassium ou un hydroxyde de sodium dans un solvant constitué de mélanges d'acétone-eau, de la cétone d'éthyle méthyle-eau ou des mélanges de ceux-ci.

3. Procédé selon la revendication 2, caractérisée en ce que le 2-{benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}-1-(4-hydroxy-phényle)-propan-1-one est isolé par cristallisation à partir de l'acétone, de la cétone d'éthyle méthyle, des mélanges d'acétone-eau, de la cétone d'éthyle méthyle-eau ou des mélanges de ceux-ci.

4. Procédé selon la revendication 1, caractérisé en ce que la salification se produit en utilisant de l'acide chlorhydrique, sous forme gazeuse ou en solution, dans un solvant organique, dans laquelle le solvant organique est du toluène ou de l'éthanol ou du méthanol ou de l'eau ou de l'acétone ou de la cétone d'éthyle méthyle ou de l'acétate d'éthyle ou des mélanges de ceux-ci.

5. Procédé selon la revendication 1, caractérisé en ce que l'hydrogénation catalytique de chlorhydrate de 2- benzyle-[2-(4-benzyloxyphényle[-éthyle]-amino -1-(4-hydroxy-phényle)-propan-1-one se produit en utilisant un catalyseur constitué par du palladium sur carbone (Pd/C) dans un solvant organique, dans laquelle le solvant organique est un alcool ou un alcool mélangé avec de l'eau, dans une atmosphère d'hydrogène compris entre 2 et 12 bars, à des températures comprises entre 20°C et 45°C.

6. Composé de 2-{benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}-1-(4-hydroxy-phényle)-propan-1-one ou son sel de chlorhydrate.

7. Composé de 4-(2{benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}-propionyle)-méthanesulfonate de phényle.

8. Composé selon la revendication 6, de formule : chlorhydrate de 2-{benzyle-[2-(4-benzyloxyphényle)-éthyle]-amino}--1-(4-hydroxy-phényle)-propan-1-one.